Insight into a Bentonite-Based Hydrogel for the Conservation of Sandstone-Based Cultural Heritage: In Situ Formation, Reinforcement Mechanism, and High-Durability Evaluation

Conservation of sandstone-based cultural heritage has attracted a great deal of interest. We propose herein a novel protecting strategy, via in situ fabrication of bentonite-based hydrogels (B-H) inside sandstones, where the bentonite-based hydrogels serve as the underlying cement. To create bentonite-based hydrogels with controllable structure, possessing good mechanical and anti-swelling properties, we have optimized forming time, appearance, and viscosity. The hydrogel precursor penetrated into the pores of the sandstone; the hydrogel would then form within 3–5 h. As found by employing a fluorescent tracer, the precursor remained controllably in place without any apparent change in the sandstone morphology. The bentonite-based hydrogels that formed inside the sandstones presented strong hydrogen bonding, coordination, and ionic bonding, as well as strong mechanical interlocking to the sandstone matrix. As a result, the sandstones possessed enhanced mechanical compressive strength and excellent resistance to acid, salt, and freeze–thaw cycles. Our approach provides for a non-destructive, eco-friendly, easy-to-use, and long-term strategy for cultural preservation, one with excellent protection effects

Insight into the Ligand-Mediated Synthesis of Colloidal CsPbBr₃ Perovskite Nanocrystals: The Role of Organic Acid, Base, and Cesium Precursors

While convenient solution-based procedures have been realized for the synthesis of colloidal perovskite nanocrystals, the impact of surfactant ligands on the shape, size, and surface properties still remains poorly understood, which calls for a more detailed structure–morphology study. Herein we have systematically varied the hydrocarbon chain composition of carboxylic acids and amines to investigate the surface chemistry and the independent impact of acid and amine on the size and shape of perovskite nanocrystals. Solution phase studies on purified nanocrystal samples by ¹H NMR and IR spectroscopies have confirmed the presence of both carboxylate and alkylammonium ligands on surfaces, with the alkylammonium ligand being much more mobile and susceptible to detachment from the nanocrystal surfaces during polar solvent washes. Moreover, the chain length variation of carboxylic acids and amines, ranging from 18 carbons down to two carbons, has shown independent correlation to the size and shape of nanocrystals in addition to the temperature effect. We have additionally demonstrated that employing a more soluble cesium acetate precursor in place of the universally used Cs₂CO₃ results in enhanced processability without sacrificing optical properties, thus offering a more versatile recipe for perovskite nanocrystal synthesis that allows the use of organic acids and amines bearing chains shorter than eight carbon atoms. Overall our studies have shed light on the influence of ligand chemistry on crystal growth and stabilization of the nanocrystals, which opens the door to functionalizable perovskite nanocrsytals through surface ligand manipulation

Nanorod Suprastructures from a Ternary Graphene Oxide–Polymer–CsPbX₃ Perovskite Nanocrystal Composite That Display High Environmental Stability

Despite the exceptional optoelectronic characteristics of the emergent perovskite nanocrystals, the ionic nature greatly limits their stability, and thus restricts their potential applications. Here we have adapted a self-assembly strategy to access a rarely reported nanorod suprastructure that provide excellent encapsulation of perovskite nanocrystals by polymer-grafted graphene oxide layers. Polyacrylic acid-grafted graphene oxide (GO-<i>g</i>-PAA) was used as a surface ligand during the synthesis of the CsPbX₃ perovskite nanocrystals (NCs), yielding particles (5–12 nm) with tunable halide compositions that were homogeneously embedded in the GO-<i>g</i>-PAA matrix. The resulting NC-GO-<i>g</i>-PAA exhibits a higher photoluminescence quantum yield than previously reported encapsulated NCs while maintaining an easily tunable bandgap, allowing for emission spanning the visible spectrum. The NC-GO-<i>g</i>-PAA hybrid further self-assembles into well-defined nanorods upon solvent treatment. The resulting nanorod morphology imparts extraordinary chemical stability toward protic solvents such as methanol and water and much enhanced thermal stability. The introduction of barrier layers by embedding the perovskite NCs in the GO-<i>g</i>-PAA matrix, together with its unique assembly into nanorods, provides a novel strategy to afford robust perovskite emissive materials with environmental stability that may meet or exceed the requirement for optoelectronic applications

General Strategy for the Preparation of Stable Luminous Nanocomposite Inks Using Chemically Addressable CsPbX₃ Peroskite Nanocrystals

The potential optoelectronic applications of perovskite nanocrystals (NCs) are primarily limited by major material instability arising from the ionic nature of the NC lattice. Herein, we introduce a facile and effective strategy to prepare extremely stable CsPbX₃ NC–polymer composites. NC surfaces are passivated with reactive methacrylic acid (MA) ligands, resulting in the formation of homogeneous nanocubes (abbreviated as MA-NCs) with a size of 14–17 nm and a photoluminescence quantum yield above 80%. The free double bonds on the surface then serve as chemically addressable synthetic handles, enabling UV-induced radical polymerization. Critically, a bromide-rich environment is developed to prevent NC sintering. The composites obtained from copolymerizing MA-NCs with hydrophobic methyl methacrylate and methacrylisobutyl polyhedral oligomeric silsesquioxane monomers exhibit enhanced properties compared to previously reported encapsulated NCs, including higher quantum yields, remarkable chemical stability toward water, and much enhanced thermal stability. The good solubility of the composite in organic solvent further enables its use as a solution-processable luminescent ink, used here for fabrication of white-light-emitting diodes with high luminous efficiency and excellent color-rendering index. The resulting fluorescent and stable NC ink opens the door to potential scalable and robust optoelectronic applications